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A Randomised Controlled Trial of Subacromial Local Anaesthetic Delivery Following Rotator Cuff Surgery (SALAD Trial)

Phase 4
Conditions
Rotator Cuff Repair
Anaesthesiology - Pain management
Musculoskeletal - Other muscular and skeletal disorders
Surgery - Other surgery
Injuries and Accidents - Other injuries and accidents
Registration Number
ACTRN12623001091695
Lead Sponsor
Sydney Local Health District
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot yet recruiting
Sex
All
Target Recruitment
96
Inclusion Criteria

Patients undergoing primary unilateral shoulder surgery for rotator cuff repair with or without adjunct bony procedures (subacromial decompression, distal clavicle excision)
Patients aged greater than or equal to 18 years of age
American Society of Anesthesiologists (ASA) physical status I to III

Exclusion Criteria

Undergoing revision surgery
Contraindication to local anaesthetic administration
Co-existent coagulopathy
Chronic opioid use
Cognitive impairment such that a patient is unable to independently consent to participate

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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